A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704266



Internal ID15440918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:25432967..25433236hg38UCSC Ensembl
Innerchr16:25444288..25444557hg19UCSC Ensembl
Innerchr16:25351789..25352058hg18UCSC Ensembl
Innerchr16:25351789..25352058hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38270
hg19270
hg18270
hg17270
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527775
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704266
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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